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HCID 70981446, 화합물 → HCID 86724015, 화합물

HRID 1475424
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HRID 1475424 반응식
C(OC([N:8]1[C:16]2[C:11](=[CH:12][C:13]([C:18]3[O:22][N:21]=[C:20]([CH3:23])[N:19]=3)=[C:14]([Cl:17])[CH:15]=2)[C:10]([CH3:25])([CH3:24])[CH2:9]1)=O)(C)(C)C>C(O)(C(F)(F)F)=O.C(Cl)Cl>[Cl:17][C:14]1[CH:15]=[C:16]2[C:11]([C:10]([CH3:24])([CH3:25])[CH2:9][NH:8]2)=[CH:12][C:13]=1[C:18]1[O:22][N:21]=[C:20]([CH3:23])[N:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 70981446HCID 70981446, 화합물

생성물 1

HCID 86724015HCID 86724015, 화합물수율 89.6%

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 6422Trifluoroacetic acid용매

실험 절차

6-Chloro-3,3-dimethyl-5-(3-methyl-[1,2,4]oxadiazol-5-yl)-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester (36 mg, 0.11 mmol) was dissolved in 50% TFA in DCM (0.534 mL) and the mixture was stirred for 30 minutes and concentrated. The residue was dissolved in methanol, loaded onto an SCX column and eluted with methanol then 2.0M ammonia in methanol to release the amine and fractions concentrated, to give the title compound (26 mg), MS: [M+H]+=264.

후처리

  1. concentrationconcentrated
  2. dissolutionThe residue was dissolved in methanol
  3. washeluted with methanol
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-14f86ac442fd48cda8cb70f215e0a914
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09018214B2

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